Difference between revisions of "Ethyl acrylate"

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A colorless, acrid smelling liquid primarily used as a monomer for the production as [[acrylic resin|acrylic]] polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most [[solvent|solvents]]. Ethyl acrylate monomer is used in water [[emulsion]] paints and for coatings on [[textile|textiles]], [[paper]], and [[leather]].
 
A colorless, acrid smelling liquid primarily used as a monomer for the production as [[acrylic resin|acrylic]] polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most [[solvent|solvents]]. Ethyl acrylate monomer is used in water [[emulsion]] paints and for coatings on [[textile|textiles]], [[paper]], and [[leather]].
 
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[[[SliderGallery rightalign|ethyl acrylate.jpg~Chemical structure]]]
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'éthyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)
 
2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'éthyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)
  
[[[SliderGallery rightalign|ethyl acrylate.jpg~Chemical structure]]]
 
  
== Other Properties ==
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==Physical and Chemical Properties==
  
 
Soluble in ethanol, ether.
 
Soluble in ethanol, ether.
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|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| -72
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| -72 C
 
|-
 
|-
 
! scope="row"| Density
 
! scope="row"| Density
| 0.9405
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| 0.9405 g/ml
 
|-
 
|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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|-
 
|-
 
! scope="row"| Boiling Point
 
! scope="row"| Boiling Point
| 99.4
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| 99.4 C
 
|}
 
|}
  
== Hazards and Safety ==
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== Risks ==
  
 
Toxic by ingestion, inhalation and skin contact. Skin contact will cause irritation.  Suspected carcinogen. Flammable. Flash point = 9C   
 
Toxic by ingestion, inhalation and skin contact. Skin contact will cause irritation.  Suspected carcinogen. Flammable. Flash point = 9C   
  
LINK: [http://www.cdc.gov/niosh/ipcsneng/neng0267.html International Chemical Safety Card]
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==Resources and Citations==
 
 
== Authority ==
 
  
 
* ''The Merck Index'', Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996  Comment: entry 3805
 
* ''The Merck Index'', Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996  Comment: entry 3805

Latest revision as of 13:59, 5 August 2022

Description

A colorless, acrid smelling liquid primarily used as a monomer for the production as acrylic polymers. Ethyl acrylate self-polymerizes at room temperature and occurs more rapidly with the aid of elevated temperatures, light, or peroxides. Polyethyl acrylate is a transparent, slightly elastic resin that is resistant to most solvents. Ethyl acrylate monomer is used in water Emulsion paints and for coatings on textiles, Paper, and Leather.

Chemical structure

Ethyl acrylate.jpg

Synonyms and Related Terms

2-propenoic acid ethyl ester; acrylic acid ethyl ester; acrilato de etilo (Esp.); 2-propenoato de etilo (Esp.); acrylate d'éthyle (Fr.); etil acrilato (It.); acrilato de etilo (Port.)


Physical and Chemical Properties

Soluble in ethanol, ether.

Composition CH2:CHCOOC2H5
CAS 140-88-5
Melting Point -72 C
Density 0.9405 g/ml
Molecular Weight mol. wt. = 100.1
Boiling Point 99.4 C

Risks

Toxic by ingestion, inhalation and skin contact. Skin contact will cause irritation. Suspected carcinogen. Flammable. Flash point = 9C

Resources and Citations

  • The Merck Index, Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996 Comment: entry 3805
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993